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4 results
  1. Nonsyndromic Hearing Loss and Deafness, Mitochondrial - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1422
    ... 1494C>T pathogenic variant was 31.7% when aminoglycoside-induced deafness was included and 17.5% when it was ... for detection of five known mutations associated with aminoglycoside-induced deafness. BMC Med Genet. 2009; 10 :2. [ PMC free ...
  2. TRMU Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK591557
    ... G (a variant known to be associated with aminoglycoside-induced deafness). This modifier effect has been reported in multiple ...
  3. Nonsyndromic hearing loss 
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss
    ... ClinicalTrials.gov DEAFNESS, AUTOSOMAL DOMINANT 7; DFNA7 DEAFNESS, AMINOGLYCOSIDE-INDUCED DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2 DEAFNESS, AUTOSOMAL DOMINANT 4A; ...
  4. Genetic Hearing Loss Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1434
    ... and developmental origin. Definitions of hearing loss and deafness Hearing loss. Auditory phenotype characterized by any degree ... child and an otherwise negative family history of deafness have an 18% empiric probability of deafness in ...